A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1147147



Internal ID16000333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135584977..135590607hg38UCSC Ensembl
Innerchr9:138476823..138482453hg19UCSC Ensembl
Innerchr9:137616644..137622274hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385631
hg195631
hg185631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615891
Supporting Variants
Samples
Known GenesLOC100130954
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1147147
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer